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Q47705355-D147FB71-98F6-4E96-AD25-4800803B2F6F
Q47705355-D147FB71-98F6-4E96-AD25-4800803B2F6F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47705355-D147FB71-98F6-4E96-AD25-4800803B2F6F
Exome sequencing in a family with intellectual disability, early onset spasticity, and cerebellar atrophy detects a novel mutation in EXOSC3.
P1433
Q47705355-D147FB71-98F6-4E96-AD25-4800803B2F6F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47705355-D147FB71-98F6-4E96-AD25-4800803B2F6F
rank
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type
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Statement
wasDerivedFrom
952cb5e58d9c8ca3c86bff187c477eaf7ccc07fb
P1433
Neurogenetics